Non-aqueous electrolyte secondary battery

ABSTRACT

A non-aqueous electrolyte secondary battery has a positive electrode having a positive electrode collector, on which a positive electrode active material layer containing a positive electrode active material as a complex oxide of Li and transition metals are formed, and a negative electrode having a negative collector, on which a negative electrode active material layer is formed. The non-aqueous electrolyte secondary battery is a gel or solid non-aqueous electrolyte secondary battery having a battery device in which a positive electrode and a negative electrode are laminated with an electrolyte layer therebetween in a film-state packaging member constructed by metal foil laminated films, and containing a lithium salt, a non-aqueous solvent, and a polymer material. The concentration in mass ratio of a free acid in the electrolyte layer is 60 ppm and less. Average particle diameter of the positive electrode active material lies in a range from 10 to 22 μm, the minimum particle diameter is 5 μm or larger, the maximum particle diameter is 50 μm or smaller, and specific surface of the positive electrode active material is 0.25 m 2 /g or smaller. Lithium carbonate (Li 2 CO 3 ) contained in the positive electrode active material is 0.15 percent by weight and less. Moisture contained in the positive electrode active material is 300 ppm and less.

RELATED APPLICATION DATA

The present application claims priority to Japanese Applications Nos.P2000-102624 filed Apr. 4, 2000, P2000-108412 filed Apr. 10, 2000, andP2000-111044 filed Apr. 12, 2000, which applications are incorporatedherein by reference to the extent permitted by law.

BACKGROUND OF THE INVENTION

The present invention relates to a battery in which a battery devicehaving electrolyte as well as a positive electrode and a negativeelectrode is sealed in a film-state packaging member.

In recent years, a secondary battery used as a power source of aportable electronic device has been actively studied and developed.Among the secondary batteries, attention is paid on a lithium secondarybattery and a lithium ion secondary battery as secondary batteriescapable of realizing high energy density. Conventionally, each of eachsecondary batteries is generally constructed by interposing a liquidelectrolyte (hereinbelow, also called electrolyte solution) obtained bydissolving a lithium salt into a nonaqueous solvent between a positiveelectrode and a negative electrode and accommodating them in a housingmade of a metal.

When a hard case cell made of a metal is used, a problem such thatstrong recent demands of a lighter, smaller, and thinner secondarybattery are not sufficiently addressed occurs. As electronic devices arebecoming smaller and smaller, a secondary battery is also demanded tohave an increased degree of freedom in shape. When a metal hard casecell is used, the demand regarding shape cannot be also sufficientlyaddressed.

In order to prevent leakage of the electrolyte solution, it is necessaryto use a metal hard case cell (a positive electrode cover and a negativeelectrode can) having rigidity. As described above, when the non-aqueoussolution is used, a problem such as leakage occurs. It is thereforeproposed to use, in place of the electrolyte solution, a gel electrolyteobtained by making a non-aqueous electrolyte solution containing alithium salt held by a polymer compound, a solid electrolyte obtained bydispersing or mixing a lithium salt into a polymer compound having ionconductivity, or an electrolyte in which a lithium salt is held by asolid inorganic conductor. This non-aqueous gel polymer secondarybattery has a positive electrode having a positive electrode collectoron which a positive electrode active material layer is formed, and anegative electrode having a negative electrode collector on which anegative electrode active material is formed and has a structure that agel layer containing an electrolyte is sandwiched between the positiveelectrode active material layer of the positive electrode and thenegative electrode active layer of the negative electrode.

In the gel layer containing the electrolyte in such a non-aqueous gelpolymer secondary battery, an electrolyte solution is held in a gelmatrix. By using the gel or solid electrolyte, the problem of leakage ofthe electrolyte solution is solved. The hard case cell becomesunnecessary. The degree of freedom in shape can be increased by using afilm more flexible than a metal housing or the like as a packagingmember. Further reduction in size, weight, and thickness can berealized.

In the case of using a film-state case such as a laminated film, apolymer film, or a metal film obtained by covering metal foil made ofaluminum or the like with a resin as a packaging member, however, whenlithium hexafluorophosphate (LiPF₆), lithium tetrafluoroboric acid(LiBF₄), or the like is used as a lithium salt, a problem such as abattery expansion occurs. One of the factors of this phenomenon may beconsidered that, even if a very small amount of moisture exists in abattery system, a lithium salt is descomposed and a free acid componentsuch as hydrogen fluoride (HF) or ion fluoride is generated. When thefree acid component reacts with the lithium to form lithium fluoride(LiF) or the like and the lithium in the battery system is consumed,problems such that shelf stability or charge/discharge cyclecharacteristic deteriorates and a theoretical battery capacity cannot beobtained, occur.

In a conventional secondary battery using non-aqueous gel electrolyte orsolid electrolyte, lithium-cobalt complex oxide is used as a positiveelectrode active material. A secondary battery using a non-aqueous gelelectrolyte or solid electrolyte housed in a metal foil laminate casehas a significant challenge to suppress expansion which is seen in ahigh temperature storage test or the like since a housing foraccommodating the aluminum laminate pack may be broken due to theexpansion.

In a conventional non-aqueous lithium ion secondary battery, thepositive electrode active material contains from 0.8% to 1.2% oflithium. carbonate (Li₂CO₃) so as to provide the function of generatingCO₂ gas to shut down a safety valve in the case where the temperature ofthe battery becomes high when heated or excessively charged. Aconventionally used positive electrode active material includes about500 ppm of water content by which a gas is generated when the battery isheated or excessively charged.

On the other hand, a non-aqueous gel polymer secondary battery hasimproved safety against heating and excessive charging, and it isunnecessary to generate a gas when the temperature becomes high. Theconventional non-aqueous gel polymer secondary battery useslithium-cobalt complex oxide as a positive electrode active material. Anon-aqueous gel polymer secondary battery using a metal foil laminatepack obtained by covering metal foil such as aluminum foil with a resinhas a significant challenge to suppress expansion, which is seen in ahigh temperature storage test or the like since there is the possibilitythat an aluminum laminate pack is not housed in a set case due to theexpansion.

SUMMARY OF THE INVENTION

The invention has been achieved in consideration of the problems and itsobject is to provide a battery capable of suppressing shape change andsuppressing deterioration in battery characteristics.

Another object of the invention is to provide a positive electrodeactive material capable of suppressing expansion of a battery and anon-aqueous electrolyte secondary battery using the positive electrodeactive material.

According to first aspect of the invention, a non-aqueous electrolytesecondary battery includes a battery device having a positive electrodehaving a collector, on which a positive electrode active material layercontaining a positive electrode material is formed, a negativeelectrode, and an electrolyte layer, the battery device being sealed ina film-state packaging member, and concentration in mass ratio of a freeacid in the electrolyte layer is 60 ppm and less. In the battery, morepreferably, the positive electrode active material is a composite oxideLiC_(O)O₂.

As the packaging member, preferably, a metal foil laminate case orlaminated film obtained by coating metal foil with a resin and havingthe structure of packaging resin layer/metal layer/sealant layer isused.

According to the second aspect of the invention, a non-aqueouselectrolyte secondary battery comprises a positive electrode having apositive electrode collector on which a positive electrode activematerial layer containing a positive electrode material is formed, anegative electrode having a negative electrode collector on which anegative electrode active material layer is formed, and a film-statecase as a packaging member. In the battery, average particle diameter ofthe positive electrode active material lies in a range from 10 to 22 μm.

More preferably, the positive electrode active material has minimumparticle diameter of 5 μm or larger, maximum particle diameter of 50 μmand less, and specific surface area of 0.25 m²/g and less. Preferably,the positive electrode active material is LiC_(O)O₂.

According to a third aspect of the invention, a non-aqueous electrolytesecondary battery comprises a positive electrode having a positiveelectrode collector, on which a positive electrode active material layercontaining a positive electrode material is formed, a negative electrodehaving a negative electrode collector on which a negative electrodeactive material layer is formed, and a film-state case as a packagingmember. In the battery, the positive electrode active material layercontains 0.15 percent by weight of carbonate compound. Preferably,moisture contained in the positive electrode active material is 300 ppmand less. Preferably, the positive electrode active material layer ismade of a lithium and a transition metal complex oxide LiMO₂ (where, Mis at least one material selected from Co, Ni, and Mn. More preferably,the positive electrode active material layer is made of LiCoO₂, and thecarbonate contained in the positive electrode active material is LiCoO₃.

In the non-aqueous electrolyte secondary battery according to the firstaspect of the invention, since the concentration in mass ratio of a freeacid in the electrolyte is 60 ppm and less, even when the film-statepackaging member is used, a change in shape is suppressed, anddeterioration in battery characteristics is suppressed.

In the non-aqueous electrolyte secondary battery according to the secondaspect of the invention, since the average particle diameter of thepositive electrode active material lines in a range from 10 to 22 μm,the specific surface area of the positive electrode active materialbecomes narrow, a reaction area decreases and, as a result, generationof gas when the battery is stored at high temperature, is suppressed.

In the non-aqueous electrolyte secondary battery according to the thirdaspect of the invention, since the carbonate contained in the positiveelectrode active material is 0.15 percent by weight and less,decomposing reaction when the battery is stored at high temperature issuppressed, and generation of gas is suppressed.

Other and further objects, features and advantages of the invention willappear more fully from the following description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view showing the configuration of a secondarybattery according to the first aspect of the invention;

FIG. 2 is an exploded perspective view of the secondary battery shown inFIG. 1;

FIG. 3 is a cross section taken along a III-III line of a battery deviceshown in FIG. 2;

FIG. 4 is a characteristic diagram showing concentration of a free acidin each of electrolytes of examples and comparative examples;

FIG. 5 is a characteristic diagram showing discharge capacity of asecondary battery in each of examples and comparative examples; and

FIG. 6 is a perspective view showing the configuration of a non-aqueouselectrolyte secondary battery according to second and third aspects ofthe invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Embodiments of the invention will be described in detail hereinbelowwith reference to the drawings.

FIG. 1 shows the appearance of a secondary battery according to anembodiment of the invention. FIG. 2 is an exploded view of the secondarybattery shown in FIG. 1. In the secondary battery, a battery device 20to which a positive electrode lead 11 and a negative electrode lead 12are attached is sealed in a film-state packaging member 30 (film-statecase such as a laminated film in which metal foil such as aluminum foiland the like is coated with a resin, a polymer film, or a metal film).

FIG. 3 is a cross section taken along a III-III line of a sectionalstructure of the battery device 20 in FIG. 2.

The battery device 20 is a obtained by laminating a positive electrode21 and a negative electrode 22 with, for example, a gel-stateelectrolyte layer 23 and a separator 24 in-between and rolling thelaminated body. The outermost peripheral portion of the negativeelectrode 22 is protected by a protection tape 25.

The positive electrode 21 has, for example, a positive electrodecollector layer 21 a and a positive electrode mixture layer 21 b whichis provided on one side or both sides of the positive electrodecollector layer 21 a. The positive electrode mixture layer 21 b is notprovided at one of the ends in the longitudinal direction of thepositive electrode collector layer 21 a, and there is a portion wherethe positive electrode collector layer 21 a is exposed. The positiveelectrode lead 11 is attached to the exposed portion.

The positive electrode collector layer 21 a is made of metal foil suchas aluminum (Al) foil, nickel (Ni) foil, or stainless steel foil. Thepositive electrode mixture layer 21 b contains, for example, a positiveelectrode material, a conducting agent such as carbon black or graphite,and a binder such as polyvinylidene fluoride. Preferable positiveelectrode materials are, for example, a metallic oxide, a metallicsulfide, and a specific polymer material. One or more of the materialsis/are selected according the application of the battery. To increaseenergy density, the most preferable material is a lithium compositeoxide containing LixMO2 as a main component. In the composition formula,M denotes one or more kinds of transition metal(s). Particularly, atleast one of cobalt (Co), nickel (Ni), and manganese (Mn) is preferable.The value (x) varies according to a charge/discharge state of thebattery and usually satisfies 0.05≦x≦1.12. Examples of such lithiumcomposite oxide are LiNiyCo1-yO₂ (where, 0≦y≦1) and LiMn₂O₄.

The negative electrode 22 has, for example, in a manner similar to thepositive electrode 21, a negative electrode collector layer 22 a and anegative a positive electrode mixture layer 21 b which is provided onone side or both sides of the negative electrode collector layer 22 a.The negative electrode mixture layer 22 b is not provided at one of theends in the longitudinal direction of the negative electrode collectorlayer 22 a, and there is a portion where the negative electrodecollector layer 22 a is exposed. The negative electrode lead 12 isattached to the exposed portion.

The negative electrode collector layer 22 a is made of metal foil suchas copper (Cu) foil, nickel foil, or stainless steel foil. The negativeelectrode mixture layer 22 b contains, for example, one or more ofnegative electrode materials capable of occluding and releasing alithium metal or lithium.

Negative electrode materials capable of occluding and releasing lithiumare metals and semiconductors each can form an alloy or compound withlithium, and alloys and compounds of the metals and semiconductors. Eachof the metals, alloys, and compounds is expressed by the chemicalformula DsEtLiu. In the chemical formula, D denotes at least one of ametal element and a semiconductor element capable of forming an alloy orcompound with lithium, and E denotes at least one of a metal element anda semiconductor element other than lithium and D. Each of values s, t,and u satisfies s>0, t≧0, and u≧0.

Among the metal or semiconductor elements each can form an alloy orcompound with lithium, Group 4B metal and semiconductor elements arepreferable. More preferable elements are silicon and tin, and the mostpreferable element is silicon. Alloys and compounds of those elementsare also preferable. Examples of the alloys and compounds are SiB₄,SiB₆, Mg₂Si, Mg₂Sn, Ni₂Si, TiSi₂, MoSi₂, CoSi₂, NiSi₂, CaSi₂, CrSi₂,Cu₅Si, FeSi₂, MnSi₂, NbSi₂, TaSi₂, VSi₂, WSi₂, and ZnSi₂.

Other examples of negative electrode materials capable of occluding andreleasing lithium are carbonaceous materials, metal oxides and polymermaterials. Examples of the carbonaceous materials are pyrocarbons,cokes, graphites, glassy carbons, polymer organic compound calcinedmaterials, carbon fiber, and activated carbon. The cokes include pitchcoke, needle coke, and petroleum coke. The polymeric compound calcinedmaterial is a material obtained by calcining a polymeric material suchas phynolic resin or furan resin at an appropriate temperature so as tobe carbonated. As a metal oxide, tin oxide (SiO₂) or the like can bementioned. Examples of the polymeric materials are polyacetylene, andpolypyrrole.

The electrolyte layer 23 is composed by, for example, a lithium salt, anon-aqueous solvent for dissolving the lithium salt, and a polymermaterial. Proper lithium salts are LiPF₆, LiBF₄, LiAsF₆, LiClO₄,LiCF₃SO₃, Li(CF₃SO₂)₂N, LiC₄F₉SO₃, LiCl and LiBr. Two or more of themmay be mixed.

Appropriate non-aqueous solvents are, for example, ethylene carbonate,propylene carbonate, butylene carbonate, vinylene carbonate,γ-butyrolactone, γ-valerolactone, diethoxyethan, tetraphydrofuran,2-methyltetrahydrofuran, 1,3-dioxolane, methyl acetate, methyl propionicacid, dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate,2,4-difluoroanisole, 2,6-difluoroanisole, and 4-bromoveratrole. Two ormore kinds of the above materials may be mixed. In the case of using alaminated film which will be described hereinlater as the packagingmember 30, preferably, any of the materials boiling at 150° C. or highersuch as ethylene carbonate, propylene carbonate, butylene carbonate,γ-butyrolactone, 2,4-difluoroanisole, 2,6-difluoroanisole, and4-bromoveratrole is used. When the material is easily vaporized, thepackaging member 30 is expanded and the outer shape deteriorates.

Appropriate polymer materials are, for example, fluoride-containedpolymers such as polyvinylidene fluoride and poly(vinylidenefluoride-co-hexafluoropropylene), ether-contained polymers such aspolyacrylonitrile, acrylonitrile-butadiene rubber,acrylonitrile-butadien-styren resin, acrylonitrile polyethylene chloridediene styrene resin, acrylonitrile vinyl chloride resin, acrylonitrilemethacrylate resin, acrylonitrile acrylate resin, and polyethylen oxide,and crosslinkers of the ethyl-contained polymers, and polyethyl modifiedsiloxane. Two or more materials may be mixed. Copolymers with thefollowing materials may be also used; acrylonitrile, vinyl acetate,methyl methacrylate, butyl methacrylate, methyl acrylate, butylacrylate, itaconic acid, methyl acrylate hydroxide, ethyl acrylatehydroxide, acryl amide, vinyl chloride, and vinylidene fluoride.Further, copolymers with ethylene oxide, propylene oxide, methylmethacrylate, butyl methacrylate, methyl acrylate, and butyl acrylatemay be also used. A copolymer of vinylidene fluoride andhexafluoropropylene, and a copolymer of ethyl modified siloxane may beused. More preferably, it is made by a micro porous polyolefin film.

The separator 24 is made by, for example, a porous film made of apolyolefin-based material such as polypropylene or polyethylene or aporous film made of an inorganic material such as ceramic nonwovencloth. A structure in which two or more kinds of porous films arestacked, may be also used. More preferably, it is made by a micro porouspolyolefin film.

The positive electrode lead 11 and the negative electrode lead 12 areled from the inside of the packaging member 30 to the outside, forexample, in the same direction. A part of the positive electrode lead 11is connected to an exposed portion in the positive electrode collectorlayer 21 a in the packaging member 30. A part of the negative electrodelead 12 is connected to an exposed portion of the negative electrodecollector layer 22 a in the packaging member 30. The positive electrodelead 11 and the negative electrode lead 12 are made of a metal materialsuch as aluminum, copper, nickel, or stainless steel in a thin film ormesh state.

In the case of using a film-state case as the packaging member 30, thepackaging member 30 is constructed by, for example, two rectangularfilms 30 a and 30 b each having a thickness of about 90 μm to 110 μm.For example, the peripheral portions of the films 30 a and 30 b adheresto each other by fusion or by using an adhesive. When the packagingmember 30 (films 30 a and 30 b) takes the form of a laminated filmobtained by coating metal foil such as aluminum foil with a resin, thefollowing materials can be used. Plastic materials to be used will beabbreviated as follows: polyethylene terephthalate:PET, fusedpolypropylane:PP, casting polypropylene:CPP, polyethylene:PE,low-density polyethylene:LDPE, high-density polyethylene:HDPE, linearlow-density polyethylene:LLDPE, and nylon:Ny. Aluminum as a metalmaterial used for a permeability-resistant barrier film is abbreviatedas AL. SUS foil may be used in the same way.

The most common structure is an packaging layer/metal layer/sealantlayer=PET/AL/PE. Not only the combination but also configurations ofother general laminated films as shown below can be also used; packaginglayer/metal film/sealant layer=Ny/AL/CPP, PET/AL/CPP, PET/AL/PET/CPP,PET/Ny/AL/CPP, PET/Ny/AL/Ny/CPP, PET/Ny/AL/Ny/PE, Ny/PE/AL/LLDPE,PET/PE/AL/PET/LDPE, and PET/Ny/AL/LDPE/CPP. Obviously, the metal filmcan be also made of any of metals other than AL.

In the embodiment, a laminated film in which, for example, a nylon film,aluminum foil, and a polyethylene film are laminated in this order, isused. In the laminated film, the polyethylene film faces the batterydevice 20. The aluminum foil in the laminated film has moistureresistance for preventing intrusion of outside air. In place of thelaminated film, a laminated film having the other structure, a polymerfilm made of polypropylene or the like, or a metal film can be also usedas the packaging member 30.

As shown in FIGS. 2 and 3, the positive electrode lead 11, the negativeelectrode lead 12, and the packaging member 30 closely adheres to eachother with, for example, a film 31 in-between so as to prevent intrusionof the outside air. The film 31 is made of a material which adheres tothe positive electrode lead 11 and the negative electrode lead 12. Wheneach of the positive electrode lead 11 and the negative electrode lead12 is made of any of the above-described metal materials, preferably,the film 31 is made of a polyolefin resin such as polyethylene,polypropylene, modified polyethylene, or modified polypropylene.

A non-aqueous electrolyte secondary battery having such a structure canbe manufactured as follows.

First, a positive electrode mixture is prepared by mixing a positiveelectrode material, a conducting agent, and a binder. The positiveelectrode mixture is dispersed in a solvent of N-methyl-pyrrolidone orthe like to thereby obtain a positive electrode mixture slurry. Thepositive electrode mixture slurry is applied on one side or both sidesof the positive electrode collector layer 21 a, dried, and compressionmolded, thereby forming the positive electrode mixture layer 21 b. Insuch a manner, the positive electrode 21 is fabricated. The positiveelectrode mixture is not applied to one end of the positive electrodecollector layer 21 a but the end is exposed.

Next, a negative electrode mixture is prepared by mixing a negativeelectrode material capable of occluding and releasing lithium with abinder and dispersing the mixture in a solvent of N-methyl-pyrrolidoneor the like to thereby obtain a negative electrode mixture slurry. Thenegative electrode mixture slurry is applied on one side or both sidesof the negative electrode collector layer 22 a, dried, and compressionmolded, thereby forming the negative electrode mixture layer 21 b. Insuch a manner, the negative electrode 21 is fabricated. The negativeelectrode mixture is not applied to one end of the negative electrodecollector layer 22 a but the end is exposed.

Subsequently, the positive electrode lead 11 is attached to the exposedportion of the positive electrode collector layer 21 a by resistancewelding, ultrasonic welding, or the like, and the electrolyte is, forexample, applied on the positive electrode mixture layer 21 b to formthe electrolyte layer 23. The negative electrode lead 12 is attached tothe exposed portion of the negative electrode collector layer 22 a byelectric resistance welding, ultrasonic welding, or the like, and theelectrolyte is, for example, applied on the negative electrode mixturelayer 22 b to form the electrolyte layer 23. After that, for example,the separator 24, the positive electrode 21 on which the electrolytelayer 23 is formed, the separator 24, and the negative electrode 22 onwhich the electrolyte layer 23 is formed are sequentially laminated anda laminated product is rolled, and the outermost portion is, forexample, adhered by the protection tape 25. In such a manner, thebattery device 20 is formed.

At the time of forming the electrolyte layer 23, for example, thematerials (that is, the mixture of the lithium salt, non-aqueoussolvent, and polymer material) of the electrolyte stored in a dryatmosphere are heated to about 70° C. to be polymerized. Whilemaintaining the temperature, the resultant is applied on the positiveelectrode mixture layer 21 b or the negative electrode mixture layer 22b, thereby preventing generation of a free acid.

After forming the battery device 20, for example, the films 30 a and 30b are prepared to sandwich the battery device 20 and are contact bondedto the battery device 20 in a reduced pressure atmosphere, and the outerperipheral portions of the films 30 a and 30 b are bonded to each otherby thermal fusion bonding or the like. Films 31 are disposed so as tosandwich the positive electrode lead 11 and the negative electrode lead12 at the end portions of the films 30 a and 30 b from which thepositive electrode lead 11 and the negative electrode lead 12 are led,and the peripheries of the films 30 a and 30 b are bonded to each othervia the film 31. In such a manner, the battery shown in FIGS. 1 to 3 iscompleted.

The secondary battery acts as follows.

When the secondary battery is charged, for example, lithium ions arereleased from the positive electrode 21 and occluded by the negativeelectrode 22 via the electrolyte layer 23. When the secondary battery isdischarged, for example, the lithium ions are released from the negativeelectrode 22 and occluded by the positive electrode 21 with theelectrolyte layer 23 in-between. Since the concentration in mass ratioof a free acid in the electrolyte layer 23 is 60 ppm and less, thebattery is prevented from being expanded. The reaction between the freeacid and the lithium in the battery system is suppressed, so thatexcellent battery characteristics are attained.

In the embodiment, the concentration in mass ratio of the free acid inthe electrolyte layer 23, that is, electrolyte is 60 ppm and less. Thefree acid denotes an acid generated when the lithium salt is decomposed,and ions generated when the acid is dissociated. The free acid isgenerated due to decomposition of the lithium salt, for example, whenmoisture exists or when the electrolyte is heated. Specifically,hydrogen fluoride, fluoride ion, hydrogen chloride (HCl), chloride ion(Cl—), hydrogen bromide (HBr), bromide ion (Br—), and the like can bementioned. In the secondary battery, by suppressing the concentration ofthe free acid, generation of a gaseous hydride such as hydrogen fluoridegas and generation of a gas by corrosion reaction in the battery issuppressed, and the expansion of the battery is therefore prevented.Consumption of the lithium due to reaction between the free acid and thelithium is also suppressed, and an increase in internal resistance dueto generation of lithium fluoride is also prevented.

As described above, in the secondary battery according to theembodiment, the concentration in mass ratio of the free acid in theelectrolyte is suppressed to 60 ppm and less. Thus, generation of agaseous hydride in the battery and generation of gas by corrosionreaction in the battery can be suppressed. Consequently, a change inshape due to expansion can be prevented with the film-state packagingmember 30. In the case where the battery is stored in high-temperatureenvironment, the shape can be maintained.

The consumption of lithium due to the reaction between the free acid andthe lithium in the battery system can be also suppressed, and anincrease in the internal resistance due to generation of lithiumfluoride can be prevented. Thus, various battery characteristics such ascapacity characteristic, shelf stability, and charge/discharge cycle canbe prevented from deterioration.

A method of manufacturing a non-aqueous electrolyte secondary batteryhaving non-aqueous gel electrolyte according to the invention will nowbe described. First, a positive electrode is fabricated by forming apositive electrode active material layer on a positive electrodecollector. While heating the positive electrode to a temperatureexceeding room temperature, a gel layer containing electrolyte is formedon the positive electrode active material layer of the positiveelectrode.

The gel layer containing electrolyte may be applied on one side or oneach of both sides by a single-side coater. Specifically, the electrodeunwound from the wound role is heated by an electrode preheater. On theelectrode active material layer on one side of the electrode, acomposition for forming the gel layer containing electrolyte is appliedfrom the coater head. The applied composition for forming the gel layercontaining electrolyte is dried when passed through a dryer and becomesa gel layer containing electrolyte. The electrode on which the gel layercontaining electrolyte is formed, is taken up by the wound role.

The gel layer containing electrolyte can be also simultaneously coatedon both sides by a double-side coater. The electrode unwound from thewound role is heated by the electrode preheater, and a composition forforming the gel layer containing electrolyte is applied from the coaterhead simultaneously on both sides of the electrode active materiallayer. The applied composition for forming the gel layer containingelectrolyte is dried when passed through a dryer and becomes a gel layercontaining electrolyte. The electrode on which the gel layer containingelectrolyte is formed, is taken up by the wound role.

When pressing is necessary, for example, after forming the electrodeactive material layer and before forming the gel layer containing theelectrolyte, the electrode can be pressed by a general press roller.

In a manner similar to the case of fabricating the positive electrode,by forming a negative electrode active layer on the negative electrodecollector, the negative electrode is fabricated. Subsequently, whileheating the negative electrode to a temperature exceeding the roomtemperature, a gel layer containing electrolyte solution is formed on anegative electrode active layer of the negative electrode.

The gel layer containing electrolyte on the positive electrode side andthat on the negative electrode side adheres to each other, therebyobtaining an electrode body.

The obtained electrode body may be assembled to thereby achieving acompleted battery by any of methods such as; a method of forming a slitin the electrode on which the gel layer containing electrolyte is formedand assembling the electrode; a method of forming a slit in theelectrode first, forming the gel layer containing the electrolytesolution, and assembling the electrode; and a method as a combination ofthe methods, of forming the gel layer containing the electrolytesolution and forming a slit in one of the electrodes, forming a slit andthen forming the gel layer containing the electrolyte solution on theother electrode, and assembling the electrodes. A method of forming thegel layer containing electrolyte only one side of an electrode, forminga slit, forming the gel layer on the other face of the electrode, andassembling the electrode may be also used.

In the battery device, after leads are welded to the portions in thecollector, in which the active material layer is not applied, theelectrodes are laminated so that the active material layers of theelectrodes face each other. The electrodes may be laminated by stackingelectrodes which are cut in a desired size, winding stacked electrodes,and the like.

The battery device fabricated in such a manner is sandwiched by thelaminated films, the resultant is pressed to increase the adhesion ofthe gel layers containing electrolyte on both electrodes and is sealed,so that the battery device is not exposed to outside air. In such amanner, a non-aqueous gel polymer secondary battery using the aluminumlaminate pack as shown in FIG. 1 is obtained.

The invention is not limited to the method of preheating the electrodebefore coating the composition for forming the gel layer containingelectrolyte in the invention. A method of passing atemperature-controlled roll, a method of blowing temperature-controlledair, a method of providing an infrared ray lamp, or the like can bementioned.

EXAMPLE

Further, examples of the invention will be described in detail.

Examples 1-1 to 1-31

First, a copolymer of vinylidene fluoride and hexafluoropropylene aspolymer materials was dissolved in a solvent obtained by mixingpropylene carbonate and ethylene carbonate, and further, LiPF₆ wasdissolved as a lithium salt. The mixing ratio in volume of the solventand the polymeter material, specifically, propylene carbonate:ethylenecarbonate:copolymer was set to 4:4:1. LiPF₆ was dissolved at the rate of0.74 mol/dm³.

The mixture solution was stored in a drying chamber for one week orlonger and heated to about 70° C. so as to be gelled. In such a manner,electrolytes of the Examples 1-1 to 1-31 were obtained. The electrolytesof the Examples 1-1 to 1-31 were fabricated separately under the sameconditions.

The concentration of the free acid (hydrogen fluoride in this case) ofthe obtained electrolyte was measured. To be specific, the electrolyteis dissolved in cold water of 1.5° C. or lower so as not to behydrolyzed. After adding bromothymol blue as an indicator, acid-baceneutrization titration was carried out by using a sodium hydroxide(NaOH) solution of 0.01 mol/dm³, thereby measuring the concentration.The results are shown in FIG. 4. In FIG. 4, the vertical axis denotesconcentration (unit: ppm) in mass ratio of the free acid, and thelateral axis denotes numbers of the example and comparative exampleswhich will be described hereinlater. As shown in FIG. 4, theconcentration in mass ratio of the free acid in each of the electrolytesof the examples is 60 ppm and less.

As Comparative Examples 1-1 to 1-29 of the present examples,electrolytes were fabricated in a manner similar to the examples exceptthat the storage time in the dying chamber was set to one day and theheating temperature was set to 80 to 90° C. The concentration of thefree acid was measured with respect to each of Comparative Examples 1-1to 1-29 in a manner similar to the examples. The result is also shown inFIG. 4. As shown in FIG. 4, the concentration at mass ratio of the freeacid in each of the electrolytes in Comparative Examples 1-1 to 1-29 was70 ppm or higher.

Secondary batteries as shown in FIGS. 1 to 3 were fabricated by usingthe electrolytes of the examples and comparative examples. First, apositive electrode mixture was prepared by mixing lithium-cobalt complexoxide (LiCoO₂) as a positive electrode material, graphite as aconducting agent, and polyvinylidene fluoride as a binder. The positiveelectrode mixture was dispersed in N-methyl-pyrrolidone as a solvent tothereby obtain a positive electrode mixture slurry. The positiveelectrode mixture slurry was applied on both sides of the positiveelectrode collector layer 21 a made of aluminum foil, dried, andcompression molded, thereby forming the positive electrode mixture layer21 b. In such a manner, the positive electrode 21 was fabricated. Anegative electrode mixture was prepared by mixing graphite powders as anegative electrode material with polyvinylidene fluoride as a binder,the mixture was dispersed in a solvent of N-methyl-pyrrolidone tothereby obtain a negative electrode mixture slurry. The negativeelectrode mixture slurry was applied on both sides of the negativeelectrode collector layer 22 a made of copper foil, dried, andcompression molded, thereby forming the negative electrode mixture layer22 b. In such a manner, the negative electrode 22 was fabricated.

After forming the positive and negative electrodes, the positiveelectrode lead 11 was attached to the positive electrode collector layer21 a and the electrolyte was applied on the positive electrode mixturelayer 21 b to form the electrolyte layer 23. The negative electrode lead12 was attached to the negative electrode collector layer 22 a and theelectrolyte was applied on the negative electrode mixture layer 22 b toform the electrolyte layer 23. After that, a porous polypropylene filmas the separator 24 was prepared, and the separator 24, the positiveelectrode 21, the separator 24, and the negative electrode 22 weresequentially laminated and a laminated product was rolled. The outermostportion was adhered by the protection tape 25. In such a manner, thebattery device 20 was formed.

After forming the battery device 20, two metal foil laminated films eachobtained by laminating a nylon film, aluminum foil, and a polyethylenefilm in this order were prepared, and the battery device 20 wassandwiched by the metal foil laminated films so that the film 31 forimproving the adhesion was disposed at the end portions from which thepositive electrode lead 11 and the negative electrode lead 12 were led.After that, the laminated films were contact bonded to the batterydevice 20, and the peripheries of the metal foil laminated films werefusion bonded to each other, thereby obtaining a secondary batteryhaving a length of 62 mm, a width of 35 mm, and a thickness of about 3.8mm.

Each of the secondary batteries of examples and comparative exampleswere repeatedly charged and discharged, a change in shape after thecharging was examined, and an initial discharge capacity was measured.The charging was performed with a constant current of 250 mA until thebattery voltage reaches 4.2V and then by a constant voltage of 4.2Vuntil the total charging time reached nine hours. On the other hand, thedischarging was performed with a constant current of 250 mA until thebattery voltage reaches 3V.

As a result, a change in the shape of the battery after charging washardly seen in each of the secondary batteries of Examples 1-1 to 1-31.On the other hand, in the secondary battery of Comparative Examples 1-1to 1-29, a gas is generated between the packaging member 30 and thebattery device 20 or in the battery device 20 in almost all of them.Each of the secondary batteries was expanded to a thickness of about 4.0mm to 4.4 mm.

FIG. 5 shows the results of the initial discharge capacity. In FIG. 5,the vertical axis denotes discharge capacity (unit; mAh), and thevertical axis denotes numbers of the examples and the comparativeexamples. As understood from FIG. 5, the discharge capacity larger than565 mAh was obtained in each of Examples 1-1 to 1-31. In contrast, thedischarge capacity smaller than 535 mAh was obtained in each ofComparative Examples 1-1 to 1-20. When they are compared with each otherby using the average values, the average value of the examples is 586mAh and that of the comparative examples is 512 mAh. In the examples,the discharge capacity larger than that in the comparative examples by14.5% was obtained. Variations in the values in the examples are smallerthan those in the comparative examples. Thus, stable results werederived.

Further, each of the secondary batteries in the examples and thecomparative examples was charged and discharged for 100 cycles. Theratio of the discharge capacity in the 100^(th) cycle to that in the1^(st) cycle (that is, the capacity sustain ratio in the 100^(th) cycle)was calculated. As a result, the average value of the capacity sustainratio of Examples 1-1 to 1-31 is 95%. On the other hand, the averagevalue of the capacity sustain ratio of the comparative examples is 87%,which is lower than the average value of the examples.

That is, it was found that, in fabrication of the electrolyte, aftersufficiently drying the lithium salt, solvent, and polymer material, theelectrolyte is gelled at low temperature of about 70° C., theconcentration of the free acid in the electrolyte can be suppressed to60 ppm or lower at the mass ratio, a change in shape of the battery canbe effectively prevented, and stable and excellent capacitycharacteristics and charge/discharge cycle characteristics can beobtained.

Examples 2-1 to 2-3

As Examples 2-1 to 2-3, secondary batteries were fabricated in a mannersimilar to Examples 1-1 to 1-31 except that the concentration in massratio of the free acid in the electrolyte was changed as shown inTable 1. As Comparative Examples 2-1 to 2-3 of Examples 2-1 to 2-3,secondary batteries were fabricated in a manner similar to the examplesexcept that the concentration of the free acid in the electrolyte asshown in Table 1. TABLE 1 concentration initial capacity in mass ratiodischarge sustain of free acid capacity ratio change in (ppm) (mAh) (%)shape Example 2-1 25 582 95 hardly occurs Example 2-2 50 584 95 hardlyoccurs Example 2-3 60 571 93 hardly occurs Comparative 100 511 89expanded Example 2-1 Comparative 200 494 84 expanded Example 2-2Comparative 400 481 81 expanded Example 2-3

The concentration of the free acid in the electrolyte in each ofExamples 2-1 to 2-3 and Comparative Examples 2-1 to 2-3 was controlledby adjusting the drying time in the drying chamber and the gellingtemperature. Specifically, in Example 2-1, the drying time was set asone week and the gelling temperature was set as 70° C. In Example 2-2,the drying time was set as 5 days, and the gelling temperature was setas 70° C. In Example 2-3, the drying time was set as 5 days, and thegelling temperature was set as 75° C. In Comparative Example 2-1, thedrying time was set as one day, and the gelling temperature was set as80° C. to 90° C. In Comparative Example 2-2, there is no drying time,and the gelling temperature was set as 85° C. to 95° C. In ComparativeExample 2-3, there is no drying time, and the gelling temperature wasset as 95° C. to 105° C.

With respect to the secondary batteries of Examples 2-1 to 2-3 andComparative Examples 2-1 to 2-3, a change in shape after charging,initial discharge capacity, and capacity sustain ratio in the 100^(th)cycle were measured in a manner similar to Examples 1-1 to 1-31. Table 1shows the results. As understood from Table 1, when the concentration ofthe free acid in the electrolyte is suppressed to 60 ppm in mass ratio,a change in shape of the battery can be prevented and excellent capacitycharacteristic and charge/discharge characteristic can be achieved.

A second aspect of the invention will now be described. Obviously, theinvention is not limited to the following examples.

Example 3

(Fabrication of Positive Electrode)

Suspension of the following composition of a positive electrode activematerial layer was mixed by a disper for four hours and was coated in apattern on both sides of aluminum foil having a thickness of 20 μm. Thecoating pattern includes a coated portion having a length of 160 mm andan uncoated portion having a length of 30 mm, which are repeatedlyprovided on both sides. The start and end positions of coating on bothsides were controlled to coincide with each other. Composition ofpositive electrode active material layer parts by weight LiCoO₂ 100polyvinylidene fluoride 5 (average molecular weight: 300,000) carbonblack (average particle diameter: 15 nm) 10 N-methyl-2-pyrrolidone 100

LiCoO₂ has, as shown in Table 2, average particle diameter of 10 μm, theminimum particle diameter of 5 μm, the maximum particle diameter of 18μm, and specific surface area of 0.25 m2/g. TABLE 2 Particle sizedistribution and specific surface area of positive electrode activematerial average particle minimum diameter particle minimum (50%diameter particle particle (5% particle diameter Specific diameter)diameter) (95% particle surface area μm μm diameter) μm m²/g Example 310 5 18 0.25 Example 4 16 7 40 0.23 Example 5 22 9 50 0.21 Comparative 63 12 0.51 Example 3 Comparative 8 5 16 0.38 Example 4

The row film of which both sides are coated with the positive electrode,was pressed with linear pressure of 300 kg/cm. After the press, thethickness of the positive electrode was 100 μm and the density of thepositive electrode active material layer was 3.45 g/cc.

(Fabrication of Negative Electrode)

Suspension of the following composition of a positive electrode activematerial layer was mixed by a disper for four hours and was coated in apattern on both sides of copper foil having a thickness of 10 μm. Thecoating pattern includes a coated portion having a length of 160 mm andan uncoated portion having a length of 30 mm, which are repeatedlyprovided on both sides. The start and end positions of coating on bothsides were controlled to coincide with each other. Composition ofnegative electrode active material layer parts by weight artificialgraphite 100 (average particle diameter: 20 μm) polyvinylidene fluoride15 (average molecular weight: 300,000) N-methyl-2-pyrrolidone 200

The row sheet of which both sides are coated with the negative electrodewas pressed with linear pressure of 300 kg/cm. After the press, thethickness of the negative electrode was 90 μm and the density of thenegative electrode active material layer was 1.30 g/cc.

Formation of Gel Layer Containing Electrolyte Solution

The composition for forming the gel layer containing the electrolytesolution was mixed by a disper for one hour in a heated state at 70° C.and was coated in a pattern on the negative electrode active materiallayers on both sides of the negative electrode collector so as to have athickness of 20 μm and was coated in a pattern on the positive electrodecollector active material layers on both sides of the positive electrodecollector so as to have a thickness of 20 μm. A dryer was controlled sothat only dimethyl carbonate evaporates substantially. Composition forforming gel layer parts containing electrolyte solution by weightpoly(hexafluoropropylene-vinylidene fluoride) copolymer *1 5 dimethylcarbonate (DMC) 75 electrolyte solution (LiPF6: 1.2 mole/litter) *2 20*1: content of hexafluoropropylene = 6 parts by weight*2: solvents used for electrolyte solution: ethylene carbonate(EC)/propylene carbonate (PC)/γ-butyrolactone (GBL) = 4/3/3

At the time of forming the gel layer containing electrolyte solution,the positive and negative electrodes were heated by setting an electrodepreheater at a predetermined temperature 60° C.

The row negative electrode on which the gel layer containing theelectrolyte solution was cut into 40 mm width to fabricate a band-shapedpancake. The row positive electrode was cut into 38 mm width tofabricate a band-shaped electrode pancake.

(Fabrication of Battery)

After that, the leads were welded to both the positive and negativeelectrodes, and the positive and negative electrodes were adhered toeach other so that their electrode active material layers were incontact with each other and contact-bonded. The resultant was sent to anassembling section where the battery device was formed. The batterydevice was sandwiched so as to be covered with the laminated films. Bywelding the laminated films, the non-aqueous gel polymer secondarybattery as shown in FIG. 6 was fabricated. As described above, thenon-aqueous gel polymer secondary battery of the embodiment used analuminum laminate pack. The laminated film was obtained by stackingnylon, aluminum, and casting polypropylene (CPP) in accordance with theorder from the outside. The thickness of nylon was 30 μm, that ofaluminum was 40 μm, and that of CPP was 30 μm. The thickness of thewhole stack layers was 100 μm.

Example 4

This example is similar to Example 3 except that physical properties ofthe positive electrode active material were different. Specifically,LiCoO₂ as the positive electrode active material has, as shown in Table2, average particle diameter of 16 μm, minimum particle diameter of 7μm, maximum particle diameter of 40 μm, and specific surface area of0.23 m²/g.

Example 5

This example is similar to Example 3 except that physical properties ofthe positive electrode active material are different. Specifically,LiCoO₂ as the positive electrode active material has, as shown in Table2, average particle diameter of 22 μm, minimum particle diameter of 9μm, maximum particle diameter of 50 μm, and specific surface area of0.21 m²/g.

Comparison Example 3

This example is similar to Example 3 except that physical properties ofthe positive electrode active material are different. Specifically,LiCoO₂ as the positive electrode active material has, as shown in Table2, average particle diameter of 6 μm, minimum particle diameter of 3 μm,maximum particle diameter of 12 μm, and specific surface area of 0.51m²/g.

Comparison Example 4

This example is similar to Example 3 except that physical properties ofthe positive electrode active material are different. Specifically,LiCoO₂ as the positive electrode active material has, as shown in Table2, average particle diameter of 8 μm, minimum particle diameter of 5 μm,maximum particle diameter of 16 μm, and specific surface area of 0.38m²/g.

Examples 3 to 5 and Comparative Examples 3 and 4 fabricated as describedabove were evaluated. Evaluation items are expansion ratio and capacitysustain ratio.

First, the expansion ratio will be described. The expansion ratio of abattery was measured as follows. A plurality of batteries of theexamples and the comparative examples were prepared. Each battery wascharged under the conditions of 4.2V, 500 mA, and two hours and thirtyminutes, and the thickness of the battery was measured. After that, thebatteries were stored under the conditions of constant temperature andfixed period such that the batteries were stored at 23° C. for onemonth, 35° C. for one month, 45° C. for one month, 60° C. for one month,and 90° C. for four hours. The thickness of each of the batteries onehour after the end of storage. A variation in thickness before and afterthe storage is used as an expansion amount. The expansion ratio isdefined as follows.Expansion ratio (%)=(expansion amount/thickness of a battery beforestorage)×100The following method of measuring the thickness of a battery was used.Specifically, the battery was placed on a stand having a horizontalplane. A disc which is parallel to the plane and is larger than thesurface portion of a battery was lowered to the battery. The thicknessof the battery was measured in a state where a load of 300 g was appliedto the disc. When the surface portion of the battery was not a flatface, the highest part of the surface portion of the battery was used tomeasure thickness.

In FIG. 6, L=62 mm, W=35 mm, and D=3.8 mm. The device area is 56 mm×34mm=1904 mm². When the surface portion of a battery is a flat face,pressure to be applied on the battery is 0.16 gf/mm².

The capacity sustain ratio will now be described. First, each of thebatteries was charged with constant current and constant voltage of hourrate of 5 (0.2 C) for 15 hours to the upper limit of 4.2V and dischargedwith constant current of 0.2 C, and the discharge was finished at thefinal voltage of 2.5V. The discharge capacity was determined in such amanner and was set as 100%. After charging batteries under theabove-described charging conditions, the batteries were stored under theconditions of 23° C. for one month, 35° C. for one month, 45° C. for onemonth, 60° C. for one month, and 90° C. for four hours. The batterieswere discharged under the above-described discharging conditions. Thecharging and discharging was repeated five more times. The dischargecapacity at the fifth time was measured and is displayed in % so as tobe compared with the discharge capacity of 100%. The capacity of 100% ineach of Examples 3 to 5 and Comparative Examples 3 and 4, that is, thecapacity before storage was almost equal to each other.

The results of measurement of the expansion ratio after storage are asshown in Table 3. When the expansion ratio is 5% or lower, there is noproblem in practice. Consequently, the expansion ratio of 5% was used asa reference of evaluation. As understood from Table 3, Example 3 has theexpansion ratio ranging from 0 to 5% and proves itself excellent.Example 4 has the expansion ratio ranging from 0 to 3% and proves itselfexcellent. Example 5 has the expansion ratio ranging from 0 to 2% andproves itself excellent. In contrast, Comparative Example 3 has a highexpansion ratio of 10 to 25% except for the condition of 23° C. for onemonth. Comparative Example 4 has a high expansion ratio of 9 to 20%except for the condition of 23° C. for one month. TABLE 3 Expansionratio after storage Expansion ratio Comparative Comparative Example 3Example 4 Example 5 Example 3 Example 4 (average (average (average(average (average Condition particle = particle = particle = particle =particle = Temperature Storage 10 μm) 16 μm) 22 μm) 6 μm) 8 μm) 23° C.one month 0% 0% 0% 0% 0% 35° C. one month 3% 2% 2% 10% 9% 45° C. onemonth 3% 2% 2% 15% 12% 60° C. one month 3% 3% 2% 20% 15% 90° C. fourhours 5% 3% 2% 25% 20%

It is understood from the above that the positive electrode activematerial used for Examples 3 to 5 produces an excellent result withrespect to the expansion ratio. Specifically, in Examples 3 to 5, theaverage particle diameter of the positive electrode active material liesin a range from 10 to 22 μm. The positive electrode active material hasthe minimum particle diameter of 5 μm, the maximum particle diameter of50 μm, and the specific surface area of 0.25 m2/g and less.

It is considered that the positive electrode active materials inExamples 3 to 5 obtain excellent results with respect to the expansionratio for the following reason. The cause of expansion of a battery whenthe battery is stored at high temperature is regarded as generation ofgas. The cause of the generation of gas is considered that, due tocontact between the surface of the positive electrode active materialwith the electrolyte solution, reaction occurs on the surface, andcracked gas of CO₂ or hydrocarbon generates. Since the surface area ofthe positive electrode active material of each of Examples 3 to 5 issmaller than that of the positive electrode active material of each ofComparative Examples 3 and 4, it is presumed that due to the smallsurface area for reaction, decomposition reaction is suppressed. As aresult, the expansion of the battery based on the cracked gas issuppressed.

The results of measurement of the capacity sustain ratio after storageare as shown in Table 4. As understood from Table 4, Example 3 has thecapacity sustain ratio ranging from 94 to 98% and proves itselfexcellent. Example 4 has the capacity sustain ratio ranging from 96 to98% and proves itself excellent. Example 5 has the capacity sustainratio ranging from 97 to 98% and proves itself excellent. In contrast,Comparative Example 3 has a capacity sustain ratio of 90 to 95% which islower as compared with Examples 3 to 5. Comparative Example 4 has acapacity sustain ratio of 92 to 96% which is lower as compared withExamples 1 to 3. TABLE 4 Capacity sustain ratio after storage Capacitysustain ratio Comparative Comparative Example 3 Example 4 Example 5Example 3 Example 4 (average (average (average (average (averageCondition particle = particle = particle = particle = particle =Temperature Storage 10 μm) 16 μm) 22 μm) 6 μm) 8 μm) 23° C. one month97% 98% 98% 95% 96% 35° C. one month 96% 98% 98% 94% 95% 45° C. onemonth 95% 97% 97% 92% 93% 60° C. one month 94% 96% 98% 90% 92% 90° C.four hours 98% 98% 98% 90% 94%

It is understood from the above that the positive electrode activematerial used for Examples 3 to 5 produces an excellent result withrespect to the capacity sustain ratio after storage. Specifically, inExamples 3 to 5, the average particle diameter of the positive electrodeactive material lies in a range from 10 to 22 μm. The positive electrodeactive material has the minimum particle diameter of 5 μm, the maximumparticle diameter of 50 μm, and the specific surface area of 0.25 m2/gand less.

It is considered that the positive electrode active materials inExamples 3 to 5 obtain excellent results with respect to the capacitysustain ratio for the following reason. Since the surface area of thepositive electrode active material of each of Examples 3 to 5 is smallerthan that of the positive electrode active material of each ofComparative Examples 3 and 4, it is presumed that due to the smallsurface area for reaction, decomposition reaction is suppressed. Due toreduction in the area for reaction, speed of deterioration in thepositive electrode active material is also suppressed.

From the above, according to the second aspect of the invention, theexpansion which occurs when a non-aqueous gel or solid electrolytepolymer secondary battery using a metal foil case laminated electricalinsulator material is stored at high temperature and is a conspicuousproblem in the secondary battery can be suppressed. The dischargecapacity sustain ratio can be improved. Specifically, the positiveelectrode active material is a composite oxide made of Li and othermetal, and the average particle diameter of the positive electrodeactive material lies within the range from 10 to 22 μm, the specificsurface area is reduced, the reaction area is decreased and, as aresult, the generation of gas is suppressed when the battery is storedat high temperature. The expansion of a battery which occurs when thebattery is stored at a high temperature can be suppressed. Thus, thedischarge capacity sustain ratio can be improved.

Examples of a third aspect of the invention will be describedhereinbelow.

Example 6

(Fabrication of Positive Electrode)

Suspension of the following composition of the positive electrode activematerial layer was mixed by a disper for four hours and was coated in apattern on both sides of aluminum foil having a thickness of 20 μm. Thecoating pattern includes a coated portion having a length of 160 mm andan uncoated portion having a length of 30 mm, which are repeatedlyprovided on both sides. The start and end positions of coating on bothsides were controlled to coincide with each other. Composition ofpositive electrode active material layer parts by weight LiCoO₂ (averageparticle diameter: 10 μm) 100 polyvinylidene fluoride 5 (averagemolecular weight: 300,000) carbon black (average particle diameter: 15nm) 10 N-methyl-2-pyrrolidone 100

The above-described positive electrode active material LiCoO₂ containsone part by weight of lithium carbonate (Li₂CO₃).

The positive electrode active material LiCoO₂ contains 400 ppm ofmoisture. The moisture in the positive electrode active material LiCoO₂was reduced to 400 ppm by drying the positive electrode active materialLiCoO₂ in vacuum and controlling the drying time.

Quantitative analysis of the moisture was conducted as follows. 0.5 g ofthe sample of the positive electrode active material was extracted andheated at 250° C. to vaporize the moisture, and the content of moisturewas measured by a Karl Fischer measuring apparatus.

Quantitative analysis of the content of lithium carbonate was made asfollows. 2.0 g of the positive electrode active material was extracted,and analyzed by using the A.G.K. CO₂ analysis method (titration methoddescribed in JISR9101).

Although the moisture is also contained in other materials such as thenegative electrode material, gel, electrolyte, the moisture contained ineach of them is very little. The moisture existing in a battery can betherefore determined by controlling the moisture contained in thepositive electrode active material.

The row sheet of which both sides were coated with the positiveelectrode was pressed with linear pressure of 300 kg/cm. After thepress, the thickness of the positive electrode was 100 μm and thedensity of the positive electrode active material layer was 3.45 g/cc.

(Fabrication of Negative Electrode)

Suspension of the following composition of the negative electrode activematerial layer was mixed by a disper for four hours and was coated in apattern on both sides of copper foil having a thickness of 10 μm. Thecoating pattern includes a coated portion having a length of 160 mm andan uncoated portion having a length of 30 mm, which are repeatedlyprovided on both sides. The start and end positions of coating on bothsides were controlled to coincide with each other. Composition ofnegative electrode active material layer parts by weight artificialgraphite 100 (average particle diameter: 20 μm) polyvinylidene fluoride15 (average molecular weight: 300,000) N-methyl-2-pyrrolidone 200

The row sheet of which both sides are coated with the negative electrodewas pressed with linear pressure of 300 kg/cm. After the press, thethickness of the negative electrode was 90 μm and the density of thenegative electrode active material layer was 1.30 g/cc.

(Formation of Gel Layer Containing Electrolyte Solution)

The composition for forming the gel layer containing the electrolytesolution was mixed by a disper for one hour in a heated state at 70° C.and was coated in a pattern on the negative electrode active materiallayers on both sides of the negative electrode collector so as to have athickness of 20 μm and was coated in a pattern on the positive electrodeactive material layers on both sides of the positive electrode collectorso as to have a thickness of 20 μm. A dryer was controlled so that onlydimethyl carbonate evaporates substantially. Composition for forming gellayer parts by containing electrolyte solution weightpoly(hexafluoropropylene-vinylidene fluoride) copolymer *1 5 dimethylcarbonate (DMC) 75 electrolyte solution (LiPF6: 1.2 mole/litter) *2 20*1: content of hexafluoropropylene = 6 parts by weight*2: solvents used for electrolyte solution: ethylene carbonate(EC)/propylene carbonate (PC)/γ-butyrolactone (GBL) = 4/3/3

At the time of forming the gel layer containing electrolyte solution,the positive and negative electrodes were heated by setting an electrodepreheater at a predetermined temperature of 60° C.

The row negative electrode on which the gel layer containing theelectrolyte solution was formed, was cut into 40 mm width to fabricate anegative electrode band. The row positive electrode was cut into 38 mmwidth to fabricate a band-shaped positive electrode body.

(Fabrication of Battery)

After that, the leads were welded to both the positive and negativeelectrodes, and the positive and negative electrodes were adhered toeach other so that their electrode active material layers were incontact with each other and contact-bonded. The resultant was sent to anassembling section where the battery device was formed. The batterydevice was sandwiched so as to be covered with the metal laminatedfilms. By welding the metal laminated films, the non-aqueous gel polymersecondary battery as shown in FIG. 6 was fabricated. As described above,the non-aqueous gel polymer secondary battery of the embodiment uses analuminum laminate case. The metal laminated film was obtained bystacking nylon, aluminum, and casting polypropylene (CPP) in accordancewith the order from the outside. The thickness of nylon is 30 μm, thatof aluminum is 40 μm, and that of CPP is 30 μm. The thickness of thewhole stack layers is 100 μm.

Examples 7 to 21

Examples 7 to 21 are similar to Example 1 except for the contents of thelithium carbonate and moisture in the positive electrode activematerial.

Specifically, the content of lithium carbonate in each of Examples 7 to9 is 1 part by weight. The contents of moisture of Examples 7 to 9 are300 ppm, 200 ppm, and 100 ppm, respectively.

The content of lithium carbonate in each of Examples 10 to 13 is 0.15percent by weight. The contents of moisture of Examples 10 to 13 are 400ppm, 300 ppm, 200 ppm, and 100 ppm, respectively.

The content of lithium carbonate of each of Examples 14 to 17 is 0.07percent by weight. The contents of moisture of Examples 14 to 17 are 400ppm, 300 ppm, 200 ppm, and 100 ppm, respectively.

The content of lithium carbonate of each of Examples 18 to 21 is 0.01percent by weight. The contents of moisture of Examples 18 to 21 are 400ppm, 300 ppm, 200 ppm, and 100 ppm, respectively.

Examples 6 to 21 fabricated as described above were evaluated.Evaluation item is an expansion ratio. The expansion ratio will now bedescribed. The expansion ratio was measured as follows. First, each ofthe batteries in the examples was charged under the conditions of 4.2V,500 mA, and two hours and thirty minutes, and the thickness of thebattery was measured. After that, the batteries were stored at 90° C.for four hours. The thickness of each of the batteries one hour afterthe end of storage was measured. A variation in thickness before andafter the storage is used as an expansion amount. The expansion ratio isdefined as follows.Expansion ratio (%)=(expansion amount/thickness of a battery beforestorage)×100

The following method of measuring the thickness of a battery is used.Specifically, the battery is placed on a stand having a horizontalplane. A disc which is parallel to the plane and is larger than thesurface portion of a battery is lowered to the battery. The thickness ofthe battery was measured in a state where a load of 300 g was applied tothe disc. When the surface portion of the battery is not a flat face,the highest part of the surface portion of the battery is used tomeasure thickness.

In FIG. 6, L=62 mm, W=35 mm, and D=3.8 mm. The device area is 56 mm×34mm=1904 mm². When the surface portion of a battery is a flat face,pressure to be applied on the battery is 0.16 gf/mm².

The result of measurement of the expansion ratio after storage is asshown in Table 5. When the expansion ratio is 4% or lower, there is noproblem in practice. It is therefore desirable that the expansion ratiois 4% or lower. TABLE 5 Expansion ratio of battery Li₂CO₃ (percent byweight) 1 0.15 0.07 0.01 moisture 400 9.00% 6.80% 6.00% 4.70% (ppm) 3007.50% 4.00% 3.60% 3.00% 200 6.40% 3.50% 2.80% 2.40% 100 5.10% 2.80%2.30% 2.00%

4% of the expansion ratio is applied to the range where the content oflithium carbonate is 0.15 percent by weight, and the content of moistureis 300 ppm and less.

As described above, by controlling the contents of lithium carbonate andmoisture in the positive electrode active material, the expansion ratioof the battery can be suppressed to 4% or lower. The reason that theexpansion ratio decreases is considered as follows. In the case wherelithium carbonate is contained in the positive electrode activematerial, the lithium carbonate is decomposed by heat when the batteryis stored at high temperature and carbon dioxide is resulted. Whenmoisture exists in the positive electrode active material, reactionoccurs between the moisture and an electrolyte such as LiPF₆ to generateHF. By the action of HF, the decomposition of lithium carbonate ispromoted, and carbon dioxide is generated. The generation of carbondioxide is considered as a cause of the expansion of a battery. In theembodiment, the contents of lithium carbonate and moisture as a cause ofgeneration of carbon dioxide are reduced. Consequently, it is presumedthat occurrence of carbon dioxide is suppressed, and the expansion of abattery is accordingly suppressed.

In consideration of the above, according to the third embodiment of theinvention, the positive electrode active material is a composite oxideof Li and a transient metal, and carbonate contained in the positiveelectrode active material is equal to or lower than 0.15 percent byweight. Consequently, decomposition reaction when the battery is storedat high temperature is suppressed. Thus, expansion of the battery whenthe battery is stored at high temperature can be suppressed.

Although not specifically described here, similar effects are alsoproduced also in the case where other laminated films having structuresother than the structure in which a nylon film, aluminum foil, and apolyethylene film are sequentially laminated are used. Similar resultscan be obtained also in the case where a metal film or a polymer film isused in place of the laminated film.

Although the invention has been described by the foregoing embodimentsand examples, the present invention is not limited to the embodimentsand the examples but can be variously modified. For example, althoughthe secondary batteries each using a gel electrolyte containing lithiumsalt, a non-aqueous solvent, and a polymer material has been describedin the embodiments and examples, in place of the gel electrolyte, otherelectrolytes such as a liquid electrolyte obtained by dissolving alithium salt into a solvent, a solid electrolyte obtained by dispersinglithium salt into polyethylene glycol or a polymer compound having ionconductivity such as acrylic polymer compound may be used.

In the foregoing embodiments and examples, the two films 30 a and 30 bare used as the packaging member 30 and the battery device 20 is sealedin the two films 30 a and 30 b. It is also possible to fold a singlefilm, closely adhere the peripheries of the film, and seal the batterydevice 20 in the folded film.

Further, the secondary batteries have been described as specificexamples in the foregoing embodiments and examples. The presentinvention can be also applied to batteries of other shapes as long as afilm-state packaging member is used. In addition, although thenon-aqueous secondary batteries have been described in the foregoingembodiments and examples, the present invention can be also applied toother batteries such as primary battery.

As described above, in the battery of the invention, the concentrationin mass ratio of a free acid in a non-aqueous electrolyte is suppressedto 60 ppm. Consequently, generation of a gaseous hydride in a batteryand generation of a gas due to corrosion reaction in the battery can besuppressed. Thus, even when a film-state packaging member is used,effects such that a change in shape due to expansion can be preventedand the shape can be maintained even when the battery is stored in ahigh-temperature environment.

It is also possible to suppress consumption of an electrode reactant dueto reaction between the free acid and an electrode reactant in a batterysystem. An effect such that deterioration in battery characteristics canbe prevented is also produced.

The second aspect of the invention produces effects such that, since thepositive electrode active material is a complex oxide of Li andtransition metal, and the average particle diameter of the positiveelectrode active material lies in the range from 10 to 22 μm, theexpansion of the battery when the battery is stored at high temperaturecan be suppressed. The discharge capacity sustain ratio can be alsoimproved.

The third aspect of the invention produces effects such that, since thepositive electrode active material is a complex oxide of Li andtransition metal, and carbonate compound contained in the positiveelectrode active material is 0.15 percent by weight. Thus, expansion ofa non-aqueous electrolyte battery which occurs when the battery isstored at high temperature can be suppressed.

Obviously many modifications and variations of the present invention arepossible in the light of the above teachings. It is therefore to beunderstood that within the scope of the appended claims the inventionmay be practiced other wise than as specifically described.

1-22. (canceled)
 1. A non-aqueous electrolyte secondary batterycomprising: a battery device having a positive electrode having acollector, on which a positive electrode active material layercontaining a positive electrode material is formed, a negativeelectrode, and a non-aqueous electrolyte layer, the battery device beingsealed in a film-state packaging member, wherein: concentration in massratio of a free acid in the electrolyte layer is 60 ppm and less; theelectrolyte is made of a lithium salt and a polymer compound, in whichthe lithium salt is dissolved or mixed, and one or more polymercompounds selected from one or more polymer compounds selected from thegroup consisting of ether-based polymers which is poly(ethylene oxide)and a crosslinked of the poly(ethylene oxide), poly(methacrylate) esterpolymer, acrylate polymer, and fluorine polymer which is poly(vinylidenefluoride) and poly(vinylidene fluoride-co-hexafluoropropylene).